ABSTRACT
There are many benefits to the overall process of standardization for tests of hemostasis
and thrombosis. Nevertheless, it should also be recognized there are several specific
problems and limitations to this process, as highlighted in this review. Some of the
issues are formidable, but it is hoped that they are not insurmountable. Sometimes,
clinical pressures drive diagnostic test processes before they are formally proven
to be of clinical value. Such clinical pressures drive diagnostic changes in the hemostasis
laboratory, including the incorporation of new and emerging technologies, which in
turn drives the need for evolving and effective external quality assurance. Incorporated
into the diagnostic or test-performance process are a large number of organizations
involved in driving standardization, with the ultimate intention of improving diagnostics,
but this process will also have unintended potential for adverse outcomes. Although
this review notes many of the benefits to the process, it focuses primarily on those
negative factors that are often less obvious but still require attention and process
review.
KEYWORDS
Standardization - regulation - laboratory assessments - hemostasis testing - diagnostic
practice - quality assurance
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Dr.
Emmanuel J Favaloro
Department of Haematology, Institute of Clinical Pathology and Medical Research, SWAHS,
Westmead
New South Wales 2145, Australia
Email: emmanuel@icpmr.wsahs.nsw.gov.au